Evidence map›Paper›PMID 26487910›Full record

ArticleACS medicinal chemistry letters2015

Thioxo-dihydroquinazolin-one Compounds as Novel Inhibitors of Myeloperoxidase.

Yang Li, Thota Ganesh, Becky A Diebold, Yerun Zhu, James W McCoy, Susan M E Smith, Aiming Sun, J David Lambeth

Abstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

  1. Myeloperoxidase as a therapeutic target for oxidative damage in Alzheimer's disease.Journal of enzyme inhibition and medicinal chemistry · 2025
    Review
  2. Article
  3. 29th Annual GP2A Medicinal Chemistry Conference.Pharmaceuticals (Basel, Switzerland) · 2021
    Article
  4. Inhibition of Myeloperoxidase.Handbook of experimental pharmacology · 2021
    Article
  5. Article
  6. Article
  7. High-Throughput Screening of NOX Inhibitors.Methods in molecular biology (Clifton, N.J.) · 2019
    Article
  8. 2,3-Dihydroquinazolin-4(1RSC advances · 2018
    Review
  9. Article
  10. Redox-based therapeutics in neurodegenerative disease.British journal of pharmacology · 2017
    Review
  11. Review
  12. Role of the Vanins-Myeloperoxidase Axis in Colorectal Carcinogenesis.International journal of molecular sciences · 2017
    Review
  13. Article
  14. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Yang LiDepartment of Pathology and Laboratory Medicine, Emory University , Atlanta, Georgia 30322, United States.
Thota GaneshDepartment of Pharmacology, Emory University , Atlanta, Georgia 30322, United States.
Becky A DieboldDepartment of Pathology and Laboratory Medicine, Emory University , Atlanta, Georgia 30322, United States.
Yerun ZhuDepartment of Pathology and Laboratory Medicine, Emory University , Atlanta, Georgia 30322, United States.
James W McCoyDepartment of Pathology and Laboratory Medicine, Emory University , Atlanta, Georgia 30322, United States.
Susan M E SmithDepartment of Molecular and Cellular Biology, Kennesaw State University , Kennesaw, Georgia 30144, United States.
Aiming SunDepartment of Pathology and Laboratory Medicine, Emory University , Atlanta, Georgia 30322, United States.
J David LambethDepartment of Pathology and Laboratory Medicine, Emory University , Atlanta, Georgia 30322, United States.

Funding

NOX1 and NOX2 as Therapeutic Targets in InfluenzaR33AI102197 · NIAID · EMORY UNIVERSITY · PI LAMBETH, JOHN DAVID · 2014 to 2016
$1.4M
NIAID NIH HHS R33 AI102197
6 · The paper itself

Abstract

Myeloperoxidase (MPO) is a key antimicrobial enzyme, playing a normal role in host defense, but also contributing to inflammatory conditions including neuroinflammatory diseases such as Parkinson's and Alzheimer's. We synthesized and characterized more than 50 quinazolin-4(1H)-one derivatives and showed that this class of compounds inhibits MPO with IC50 values as low as 100 nM. Representative compounds showed partially reversible inhibition that was competitive with respect to Amplex Red substrate and did not result in the accumulation of MPO Compound II. Members of this group show promise for therapeutic development for the treatment of diseases in which inflammation plays a pathogenic role.

Indexed as

inflammationMyeloperoxidaseNADPH-oxidasetherapeuticthioxo-dihydroquinazolin-one

Identifiers

PMID26487910
PMCPMC4601060

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.